CLOTRIMAZOLE INHIBITS CELL-PROLIFERATION IN-VITRO AND IN-VIVO

被引:151
作者
BENZAQUEN, LR
BRUGNARA, C
BYERS, HR
GATTONICELLI, S
HALPERIN, JA
机构
[1] HARVARD UNIV,SCH MED,DEPT CELL BIOL,BOSTON,MA 02115
[2] BETH ISRAEL HOSP,BOSTON,MA 02115
[3] CHILDRENS HOSP,HEMATOL LAB,BOSTON,MA 02115
[4] BOSTON UNIV,SCH MED,DEPT DERMATOL,BOSTON,MA 02118
[5] MED UNIV S CAROLINA,DEPT RADIAT ONCOL,CHARLESTON,SC 29425
关键词
D O I
10.1038/nm0695-534
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Cell proliferation is critically dependent on the regulated movement of ions across various cellular compartments. The antimycotic drug clotrimazole (CLT) has been shown to inhibit movement of Ca2+ and K+ across the plasma membrane. Our results show that CLT inhibits the rate of cell proliferation of normal and cancer cell fines in a reversible and dose-dependent manner in vitro. Moreover, CLT depletes the intracellular Ca2+ stores and prevents the rise in cytosolic Ca2+ that normally follows mitogenic stimulation. In mice with severe combined immunodeficiency disease (SCID) and inoculated intravenously with MM-RU human melanoma cells, daily subcutaneous injections of CLT induced a significant reduction in the number of lung metastases. Modulation of early ionic mitogenic: signals and potent inhibition of cell proliferation both in vitro and in vivo are new and potentially useful clinical effects of CLT.
引用
收藏
页码:534 / 540
页数:7
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